Quick measurement method for evaluating antifouling capacity by using balanus albicostatus venus larva
A technology of Venus larvae and white ridge barnacles, which is applied in the direction of optical testing for defects/defects, can solve the problems of high cost, long antifouling ability detection cycle, and insufficient antifouling performance evaluation methods, and achieves simple operation and short evaluation time , the effect of reliable data
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Embodiment 1
[0013] Example 1: Characterization of Adhesives for White Ridge Barnacle Venus Larvae
[0014] (1) Cultivation of white ridge barnacle Venus larvae
[0015] Collect adult white-ridged barnacles (Balanus aibicostatus) from the intertidal zone of the sea, clean the surface of the barnacles with sterilized seawater, dry in the shade overnight, add sterilized seawater, and ventilate for about 2 hours, until barnacle larvae are found to be released Finally, the barnacle larvae were transferred to fresh seawater with a dropper. The density of the barnacle larvae was 1 / mL, and the Platymonas cordiformis was fed twice a day. The density of the Platymonas cordiformis was 3×10 5 per mL, during which the water was changed every 24 hours, the culture temperature was 25°C, and cultured for 6-9 days, the barnacle larvae developed to the stage of Venus larvae.
[0016] (2) Adhesive secretion of white-ridged barnacle Venus larvae during the reversible attachment stage
[0017] Glass sheet (...
Embodiment 2
[0018] Example 2: Evaluation of the adhesion ability of white-ridged barnacle Venus larvae on different material surfaces
[0019] Place the glass sheet, cellulose acetate film and silicone material in 3 superhydrophobic PTFE cups, add 10ml of sterilized fresh seawater to each cup, and move into 200 white-ridged barnacle Venus larvae, under dark conditions, at 25°C Cultivate for 6h. After 6 hours, the glass, cellulose acetate film and silicone samples were taken out. Gloves should be worn throughout the experimental operation to avoid leaving fingerprints on the surface of the sample.
[0020] Place the above sample in fixative solution (57g trichloroacetic acid, 17g sulfosalicylic acid, 150mL methanol, 350mL distilled water) for 30 minutes, then put it into Coomassie brilliant blue dye solution (1.25g R-250, 230mL methanol, 40ml glacial acetic acid, 230mL distilled water), staining for 40min. After 40 minutes, put the stained sample into the decolorization solution (100mL ...
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